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App-based Cognitive Training at Home (ACTH)

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Samsung Medical Center

Status

Unknown

Conditions

Healthy Volunteers, Aged

Treatments

Behavioral: Multidisciplinary prevention

Study type

Interventional

Funder types

Other

Identifiers

NCT03494699
2018-02-050

Details and patient eligibility

About

This randomized controlled trial is for investigating the effects of multidisciplinary intervention program on cognition and activity of daily living ability in community dwelling healthy elderly. The intervention consists of cognitive group training every month, daily home cognitive training using cognitive training smartphone application, record of weekly physical activity and body weight and feedback program, and alcohol and smoking cessation monitoring and feedback program. Among these interventions, app-based cognitive training at home is the major intervention in this study. The total duration of intervention is 1 year, and the tablet-based cognitive screening test and the patient-reported questionnaires to evaluate subjective memory decline, quality of life, depression, and activity of daily living are used for outcome measures.

Enrollment

400 estimated patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • literate
  • education years >= 6 years
  • not demented
  • mini-mental status examination >= 24
  • android cellular phone users
  • no significant decline in activities of daily living (Korea- Instrumental Activities of Daily Living =<5)

Exclusion criteria

  • Who has a history of major cardiovascular diseases within 3 months of study enrollment (ex. myocardial infarction, stroke)
  • Who has current illnesses that could possibly affect cognition or with anticipated life expectancy of less than 2 years (ex. end stage cancer, on chemotherapy)
  • Who has a severe hearing difficulty or visual disturbance
  • Who has a limitation in communication
  • Who was diagnosed with dementia
  • Who has a plan for immigration or move in 1.5 years after study enrollment
  • Who underwent a cognitive training within 6 months of study enrollment

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

400 participants in 2 patient groups

Intervention group
Experimental group
Treatment:
Behavioral: Multidisciplinary prevention
Control group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Duk L. Na, MD.PhD.; Hyemin Jang, MD

Data sourced from clinicaltrials.gov

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